Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
  • C07D471/08—Bridged systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/04—Centrally acting analgesics, e.g. opioids
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/20—Hypnotics; Sedatives
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P27/00—Drugs for disorders of the senses
  • A61P27/02—Ophthalmic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P27/00—Drugs for disorders of the senses
  • A61P27/02—Ophthalmic agents
  • A61P27/06—Antiglaucoma agents or miotics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
  • C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
  • C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
  • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
  • C07D487/08—Bridged systems

Definitions

• the present invention relates to therapeutically active azacyclic compounds, a method of preparing the same and to pharmaceutical compositions comprising the compounds.
• the novel compounds are useful as stimulants of the cognitive function of the forebrain and hippocampus of mammals and especially in the treatment of Alzheimer's disease.
• One of the elderly-related symptoms is a reduction of the cognitive functions.
• This symptom is especially pronounced in the patophysiological disease known as Alzheimer's disease.
• This disease is combined with, and also most likely caused by, a up to 90% degeneration of the muscarinic cholinergic neurons in nucleus basalis, which is part of substantia innominata.
• These neurons project to the prefrontal cortex and hippocampus and have a general stimulatory effect on the cognitive functions of the forebrain as well as of hippocampus, namely learning, association, consolidation, and recognition.
• muscarinic choliner- gic agonists are useful in the treatment of Alzheimer's disease and in improving the cognitive functions of elderly people. It is well known that arecoline (methyl 1-methyl- 1,2,5,6- tetrahydropyridine-3-carboxylate) is such a cholinergic agonist.
• Arecoline however has a very short biological half life and a small separation between central and peripheral muscarinic effects. Furthermore arecoline is a rather toxic compound.
• EP-A-0307142 discloses a class of thiadiazoles, substituted on one of the ring carbon atoms with a non-aromatic azacyclic or azabicyclic ring system, and substituted on the other ring carbon atom with a substituent of low lipophilicity, or a hydrocarbon substituent, which are muscarinic agonists and therefore useful in the treatment of neurological and mental illnesses and severe painful conditions.
• novel compounds of the invention are heterocyclic compounds having the formula I
• X is oxygen or sulphur; wherein G is selected from the group of azabicyclic ring systems consisting of
• R 1 and R 2 may be present at any position, including the point of attachment of the oxadiazole or thiadiazole ring, and independently are hydrogen, -OH, halogen, -NH 2 , carboxy, straight or branched C 1-5 -alkyl, straight or branched C 2-5 -alkenyl, straight or branched C 2-5 -alkynyl, straight or branched C 1-10 -alkoxy, or straight or branched C 1-5 -alkyl substituted with -OH;
• R 3 is hydrogen, straight or branched C 1-5 -alkyl, straight or branched C 2-5 -alkenyl or straight or branched C 2-5 -alkynyl; n and p independently are 0, 1, 2, 3, or 4;
• R is Y which represents hydrogen, halogen, -CN, -CHO, -OH, -OR 4 , -SR 4 , -NH 2 , -NHR 4 , -NR 4 R 5 , -NO 2 , -SOR 4 , -SO 2 R 4 , -COR 4 , -CO 2 R , -CONH 2 , -CONHR 4 , -CONR 4 R 5 ,
• R 4 and R 5 independently are straight or branched C 1-15 -alkyl, straight or branched C 2-15 -alkenyl, straight or branched C 2-15 -alkynyl, phenyl, phenoxy, benzoyl, benzyl or benzyloxycarbonyl groups optionally substituted with halogen, -CN, C 1-4 -alkyl or C 1-4 -alkoxy; or R 4 and R 5 independently are straight or branched C 1-15 -alkyl, straight or branched C 2-15 -alkenyl, straight or branched C 2-15 -alkynyl, phenyl, phenoxy, benzoyl, benzyl or benzyloxycarbonyl groups optionally substituted with halogen, -CN, C 1-4 -alkyl or C 1-4 -alkoxy; or R 4 and R 5 independently
• salts include inorganic and organic acid addition salts such as hydrochloride, hydrobromide, sulphate, phosphate, acetate, fumarate, maleate, citrate, lactate, tartrate, oxalate, or similar pharmaceutically- acceptable inorganic or organic acid addition salt.
• the compounds of this invention are also useful analgesic agents and therefore useful in the treatment of severe painful conditions.
• the compounds of this invention are useful in the treatment of glaucoma.
• the invention also relates to methods of preparing the above mentioned compounds, comprising: a) reacting a compound of formula II wherein G has the meaning defined above, is or and R 6 is H, OH or O-alkyl, with S 2 Cl 2 to form a compound of formula III
• G has the .meaning defined above and R 7 is alkyl, amino, halogen, alkoxy or alkylthio, to form a compound of formula V
• the pharmacological properties of the compounds of the invention can be illustrated by determining their capability to inhibit the specific binding of 3 H-Oxotremorine-M ( 3 H-Oxo). Birdsdall N.J.M., Hulme E.C., and
• Three different sites are labelled by 3 H-Oxo. These sites have affinity of 1.8, 20 and 3000 nM, respectively. Using the present experimental conditions only the high and medium affinity sites are determined.
• the inhibitory effects of compounds on 3 H-Oxo binding reflects the affinity for muscarinic acetylcholine receptors.
• Fresh cortex (0.1-1 g) from male Wistar rats (150-250 g) is homogenized for 5-10 s in 10 ml 20 mM Hepes pH: 7.4, with an Ultra-Turrax homogenizer. The homogenizer is rinsed with 10 ml of buffer and the combined suspension centrifuged for 15 min at 40,000 ⁇ g. The pellet is washed three times with buffer. In each step the pellet is homogenized as before in 2 ⁇ 10 ml of buffer and centrifuged for 10 min at 40,000 ⁇ g. The final pellet is homogenized in 20 mM Hepes pH: 7.4 (100 ml per g of original tissue) and used for binding assay.
• IC 50 the concentration (ng/ml) of the test substance which inhibits the specific binding of 3 H-Oxo by 50%).
• the compounds of the invention together with a conventional adjuvant, carrier, or diluent, and if desired in the form of a pharmaceutically-acceptable acid addition salt thereof, may be placed into the form of pharmaceutical compositions and unit dosages thereof, and in such form may be employed as solids, such as tablets or filled capsules, or liquids, such as solutions, suspensions, emulsions, elixirs, or capsules filled with the same, all for oral use, in the form of suppositories for rectal administration; or in the form of sterile injectable solutions for parenteral (including subcutaneous) use.
• Such pharmaceutical compositions and unit dosage forms thereof may comprise conventional ingredients in conventional proportions, with or without additional active compounds or principles, and such unit dosage forms may contain any suitable effective muscarinic cholinergic agonistic amount of the active ingredient commensurate with the intended daily dosage range to be employed.
• Tablets containing ten (10) milligrams of the active ingredient or, more broadly, one (1) to hundred (100) milligrams, per tablet, are accordingly suitable representative unit dosage forms.
• the compounds of this invention can thus be used for the formulation of pharmaceutical preparations, e.g. for oral and parenteral administration to mammals including humans, in accordance with conventional methods of galenic pharmacy.
• excipients are such pharmaceutically acceptable organic or inorganic carrier substances suitable for parenteral or enteral application which do not deleteriously react with the active compounds.
• Such carriers are water, salt solutions, alcohols, polyethylene glycols, polyhydroxyethoxylated castor oil, gelatine, lactose, amylose, magnesium stearate, talc, silicic acid, fatty acid monoglycerides and diglycerides, pentaerythritol fatty acid esters, hydroxymethylcellulose and polyvinylpyrrolidone.
• the pharmaceutical preparations can be sterilized and mixed, if desired, with auxiliary agents, emulsifiers, salt for influencing osmotic pressure, buffers and/or coloring substances and the like, which do not deleteriously react with the active compounds.
• auxiliary agents emulsifiers, salt for influencing osmotic pressure, buffers and/or coloring substances and the like, which do not deleteriously react with the active compounds.
• injectable solutions or suspensions preferably aqueous solutions with the active compound dissolved in polyhydroxylated castor oil.
• Ampoules are convenient unit dosage forms.
• a syrup, elixir of the like can be used in cases where a sweetened vehicle can be employed.
• the compounds of this invention are dispensed in unit form comprising 1-100 mg in a pharmaceuticallyacceptable carrier per unit dosage.
• the dosage of the compounds according to this invention is 1-100 mg/day, preferably 10-70 mg/day, when administered to patients, e.g. humans, as a drug.
• a typical tablet which may be prepared by conventional tabletting techniques contains:
• the compounds of the invention are extremely useful in the treatment symptoms related to a reduction of the cognitive functions of the brain of mammals, when administered in an amount effective for stimulating the cognitive functions of the forebrain and hippocampus.
• the important stimulating activity of the compounds of the invention includes both activity against the patophysiological disease, Alzheimer's disease as well as against normal degeneration of brain function.
• the compounds of the invention may accordingly be administered to a subject, e.g., a living animal body, including a human, in need of stimulation of the cognitive functions of the forebrain and hippocampus, and if desired in the form of a pharmaceutically-acceptable acid addition salt thereof (such as the hydrobromide, hydrochloride, or sulfate, in any event prepared in the usual or conventional manner, e.g., evaporation to dryness of the free base in solution together with the .acid), ordinarily concurrently, simultaneously, or together with a pharmaceutically-acceptable carrier or diluent, especially and preferably in the form of a pharmaceutical composition thereof, whether by oral, rectal, or parenteral (including subcutaneous) route, in an effective forebrain and hippocampus stimulating amount, and in any event an amount which is effective for improving the cognitive function of mammals due to their muscarinic cholinergic receptor agonistic activity.
• a pharmaceutically-acceptable acid addition salt thereof such as the hydrobro
• Suitable dosage ranges are 1-100 milligrams daily, 10-100 milligrams daily, and especially 30-70 milligrams daily, depending as usual upon the exact mode of administration, form in which administered, the indication toward which the administration is directed, the subject involved and the body weight of the subject involved, and the preference and experience of the physician or veterinarian in charge.
• the first fractions contained the exo compound, which after crystallization with oxalic acid in acetone was collected in 50 mg yield. (Compound 19). M.p. 110-112oC. The next fractions contained the endo compound, which after crystallization with oxalic acid in acetone was collected in 20 mg yield. (Compound 20). M.p. 127- 129°C.
• Exo-6-(3-Hexylthio-1,2,5-thiadiazol-4-yl)-1-azabicyclo-[3.2.1]octane oxalate To a solution of exo-6-(3-chloro-1,2,5-thiadiazol-4-yl)- 1-azabicyclo[3.2.1]octane (229 mg, 1.0 mmol) in DMF (20 ml) was added sodiumhydrogen sulfide monohydrate (230 mg, 3.0 mmol). The reaction mixture was stirred at room temperature for 1 h. Potassium carbonate (1.38 g, 10 mmol) and 1-hexylbromide (335 mg, 2.5 mmol) was added and the mixture was stirred for 1 h.
• Acetic acid (1.26 ml, 22 mmol) was added to the reaction mixture over 30 min. at 5-10oC.
• the reaction mixture was stirred at room temperature for further 18 h and cooled to 5oC.
• Aqueous sodium hydroxide was added to obtain alkaline pH and then extracted with methylene chloride (3 ⁇ 200 ml).
• the combined organic phases were evaporated and the residue was treated with a solution of ammonium chloride (3.8 g, 72 mmol) in water (10 ml) and 25% aqueous ammonia (5 ml).
• the reaction mixture was stirred at room temperature for 18 h and then extracted with methylene chloride.
• the combined organic phases were dried and evaporated to give the title compound. Yield. 1.67 g.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Medicinal Chemistry (AREA)
• General Chemical & Material Sciences (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Pharmacology & Pharmacy (AREA)
• Life Sciences & Earth Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Biomedical Technology (AREA)
• Neurology (AREA)
• Neurosurgery (AREA)
• Ophthalmology & Optometry (AREA)
• Hospice & Palliative Care (AREA)
• Psychiatry (AREA)
• Pain & Pain Management (AREA)
• Anesthesiology (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
• Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
• Plural Heterocyclic Compounds (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)
• Compounds Of Unknown Constitution (AREA)
• Preparation Of Compounds By Using Micro-Organisms (AREA)
• Lubricants (AREA)
• Hydrogenated Pyridines (AREA)

Priority Applications (12)

Applications Claiming Priority (2)

Publications (1)

Family

ID=8109272

Family Applications (1)

Country Status (23)

Cited By (35)

Families Citing this family (21)

Citations (7)

Family Cites Families (4)

• 1990
  • 1990-08-21 DK DK198590A patent/DK198590D0/da not_active Application Discontinuation
• 1991
  • 1991-08-12 IL IL99165A patent/IL99165A/xx not_active IP Right Cessation
  • 1991-08-13 US US07/744,160 patent/US5260314A/en not_active Expired - Lifetime
  • 1991-08-19 NZ NZ239450A patent/NZ239450A/en not_active IP Right Cessation
  • 1991-08-20 CA CA002089769A patent/CA2089769C/en not_active Expired - Fee Related
  • 1991-08-20 AU AU84036/91A patent/AU662105B2/en not_active Ceased
  • 1991-08-20 CZ CS93244A patent/CZ282606B6/cs not_active IP Right Cessation
  • 1991-08-20 JP JP03513857A patent/JP3100160B2/ja not_active Expired - Fee Related
  • 1991-08-20 ZA ZA916581A patent/ZA916581B/xx unknown
  • 1991-08-20 ES ES91915629T patent/ES2124707T3/es not_active Expired - Lifetime
  • 1991-08-20 SG SG1996005511A patent/SG68567A1/en unknown
  • 1991-08-20 DE DE69130570T patent/DE69130570T2/de not_active Expired - Fee Related
  • 1991-08-20 AT AT91915629T patent/ATE174027T1/de not_active IP Right Cessation
  • 1991-08-20 EP EP91915629A patent/EP0544779B1/en not_active Expired - Lifetime
  • 1991-08-20 DK DK91915629T patent/DK0544779T3/da active
  • 1991-08-20 SK SK127-93A patent/SK283219B6/sk unknown
  • 1991-08-20 KR KR1019930700496A patent/KR100247121B1/ko not_active IP Right Cessation
  • 1991-08-20 WO PCT/DK1991/000236 patent/WO1992003433A1/en active IP Right Grant
  • 1991-08-20 HU HU9300464A patent/HU221433B/hu unknown
  • 1991-08-21 IE IE296091A patent/IE912960A1/en not_active IP Right Cessation
  • 1991-08-21 PT PT98736A patent/PT98736B/pt not_active IP Right Cessation
• 1993
  • 1993-02-19 FI FI930747A patent/FI930747A/fi not_active Application Discontinuation
  • 1993-02-19 NO NO930601A patent/NO301883B1/no unknown
• 1995
  • 1995-06-29 HU HU95P/P00608P patent/HU211861A9/hu unknown
• 1999
  • 1999-02-03 GR GR990400369T patent/GR3029289T3/el unknown

Patent Citations (7)

Also Published As

Similar Documents

Legal Events